Quantitative Proteomic Analysis Reveals Impaired Axonal Guidance Signaling in Human Postmortem Brain Tissues of Chronic Traumatic Encephalopathy
- Author:
Baibin BI
1
;
Han Pil CHOI
;
Seung Jae HYEON
;
Shengnan SUN
;
Ning SU
;
Yuguang LIU
;
Junghee LEE
;
Neil W KOWALL
;
Ann C MCKEE
;
Jing Hua YANG
;
Hoon RYU
Author Information
- Publication Type:Original Article
- Keywords: Chronic traumatic encephalopathy (CTE); Quantitative proteomics; Axonal guidance; Oligodendrocyte; Neuron; Neurodegeneration
- MeSH: Axons; Blotting, Western; Brain Injury, Chronic; Brain; Cell Body; Cerebral Cortex; Craniocerebral Trauma; Cytoskeletal Proteins; Gray Matter; Humans; Immunohistochemistry; Neurodegenerative Diseases; Neurons; Neuropathology; Neuropil; Oligodendroglia; tau Proteins; White Matter
- From:Experimental Neurobiology 2019;28(3):362-375
- CountryRepublic of Korea
- Language:English
- Abstract: Chronic traumatic encephalopathy (CTE) is a distinct neurodegenerative disease that associated with repetitive head trauma. CTE is neuropathologically defined by the perivascular accumulation of abnormally phosphorylated tau protein in the depths of the sulci in the cerebral cortices. In advanced CTE, hyperphosphorylated tau protein deposits are found in widespread regions of brain, however the mechanisms of the progressive neurodegeneration in CTE are not fully understood. In order to identify which proteomic signatures are associated with CTE, we prepared RIPA-soluble fractions and performed quantitative proteomic analysis of postmortem brain tissue from individuals neuropathologically diagnosed with CTE. We found that axonal guidance signaling pathwayrelated proteins were most significantly decreased in CTE. Immunohistochemistry and Western blot analysis showed that axonal signaling pathway-related proteins were down regulated in neurons and oligodendrocytes and neuron-specific cytoskeletal proteins such as TUBB3 and CFL1 were reduced in the neuropils and cell body in CTE. Moreover, oligodendrocyte-specific proteins such as MAG and TUBB4 were decreased in the neuropils in both gray matter and white matter in CTE, which correlated with the degree of axonal injury and degeneration. Our findings indicate that deregulation of axonal guidance proteins in neurons and oligodendrocytes is associated with the neuropathology in CTE. Together, altered axonal guidance proteins may be potential pathological markers for CTE.
